A Genetically Modified Skin Graft for Treating Alcohol Use Disorder and/or Polysubstance Abuse With Cocaine.

Advances in drug and alcohol research Pub Date : 2021-06-18 eCollection Date: 2021-01-01 DOI:10.3389/adar.2021.10007
Qingyao Kong, Xiaoyang Wu, Ming Xu
{"title":"A Genetically Modified Skin Graft for Treating Alcohol Use Disorder and/or Polysubstance Abuse With Cocaine.","authors":"Qingyao Kong, Xiaoyang Wu, Ming Xu","doi":"10.3389/adar.2021.10007","DOIUrl":null,"url":null,"abstract":"<p><p>Alcohol use disorder (AUD) is one of the foremost public health problems. Alcohol is also frequently co-abused with cocaine. There is a huge unmet need for the treatment of AUD and/or cocaine co-abuse. We have developed and used a skin stem cell-based gene delivery platform and found that production of the glucagon-like peptide-1 (GLP1) from the grafted genetically modified skin reduced development and reinstatement of alcohol-induced drug-taking and seeking, voluntary oral alcohol consumption and alcohol-induced increase in dopamine (DA) levels in the nucleus accumbens (NAc). Moreover, we have developed a novel co-grafting procedure for both modified human butyrylcholinesterase (hBChE)- and GLP1-expressing cells. Skin grafts-derived hBChE and GLP1 reduced acquisition of drug-taking and toxicity induced by concurrent alcohol and cocaine injections. These results imply that gene delivery through skin transplants may add a new option to treat drug abuse and co-abuse.</p>","PeriodicalId":72092,"journal":{"name":"Advances in drug and alcohol research","volume":"1 1","pages":"10007"},"PeriodicalIF":0.0000,"publicationDate":"2021-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10880775/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in drug and alcohol research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/adar.2021.10007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Alcohol use disorder (AUD) is one of the foremost public health problems. Alcohol is also frequently co-abused with cocaine. There is a huge unmet need for the treatment of AUD and/or cocaine co-abuse. We have developed and used a skin stem cell-based gene delivery platform and found that production of the glucagon-like peptide-1 (GLP1) from the grafted genetically modified skin reduced development and reinstatement of alcohol-induced drug-taking and seeking, voluntary oral alcohol consumption and alcohol-induced increase in dopamine (DA) levels in the nucleus accumbens (NAc). Moreover, we have developed a novel co-grafting procedure for both modified human butyrylcholinesterase (hBChE)- and GLP1-expressing cells. Skin grafts-derived hBChE and GLP1 reduced acquisition of drug-taking and toxicity induced by concurrent alcohol and cocaine injections. These results imply that gene delivery through skin transplants may add a new option to treat drug abuse and co-abuse.

一种用于治疗可卡因酒精使用障碍和/或多物质滥用的转基因皮肤移植物
酒精使用障碍(AUD)是最重要的公共卫生问题之一。酒精也经常与可卡因一起被滥用。对澳元和/或可卡因共同滥用的治疗存在巨大的未满足需求。我们开发并使用了一种基于皮肤干细胞的基因传递平台,发现从移植的转基因皮肤中产生胰高血糖素样肽-1 (GLP1)减少了酒精诱导的药物摄入和寻求的发展和恢复,自愿口服酒精摄入和酒精诱导的伏隔核(NAc)多巴胺(DA)水平的增加。此外,我们已经开发了一种新的共嫁接方法,用于修饰的人丁基胆碱酯酶(hBChE)-和表达glp1的细胞。皮肤移植物衍生的hBChE和GLP1减少了酒精和可卡因同时注射引起的药物摄取和毒性。这些结果表明,通过皮肤移植的基因传递可能为治疗药物滥用和共同滥用提供了一种新的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信